search
Back to results

Influence Of Omeprazole On The Anti-Platelet Action Of Clopidogrel

Primary Purpose

Coronary Heart Disease

Status
Completed
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
impact on VASP test
Sponsored by
University Hospital, Brest
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Heart Disease focused on measuring clopidogrel, omeprazole

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: patient with indication of aspirin and clopidogrel treatment Exclusion Criteria: patient<18 years liver disease drug eluting stent gastrointestinal ulcus bleeding pregnancy

Sites / Locations

  • Department of Cardiology

Outcomes

Primary Outcome Measures

inter group comparison of VASP test

Secondary Outcome Measures

Full Information

First Posted
July 6, 2006
Last Updated
August 22, 2008
Sponsor
University Hospital, Brest
search

1. Study Identification

Unique Protocol Identification Number
NCT00349661
Brief Title
Influence Of Omeprazole On The Anti-Platelet Action Of Clopidogrel
Official Title
Influence Of Omeprazole On The Anti-Platelet Action Of Clopidogrel Associated To Aspirin: Double-Blind Randomized Trial Against Placebo
Study Type
Interventional

2. Study Status

Record Verification Date
August 2008
Overall Recruitment Status
Completed
Study Start Date
June 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University Hospital, Brest

4. Oversight

5. Study Description

Brief Summary
Objectives: A prospective investigation of the effect of omeprazole, a proton pump inhibitor, on the anti-platelet action of clopidogrel. The main decision criterion will concern change in VASP protein phosphorylation under treatment. Phosphorylation will be measured before and after administration of omeprazole versus placebo in patients undergoing clopidogrel treatment. Type of study: Single center, double blind, randomized parallel group study versus placebo, comparing two treatment groups: clopidogrel + omeprazole + standard regime (beta-blockers, atorvastatin, IEC, aspirin) clopidogrel + placebo+ standard regime (beta-blockers, atorvastatin, IEC, aspirin) Study population: 120 patients from the Cardiology Department of Brest University hospital, Brest (France), receiving a standard treatment comprising a loading dose of clopidogrel followed by a daily dose of 75 mg associated to 75 mg aspirin, will be randomized between 20 mg/day omeprazole and 20 mg/day placebo treatment groups. The efficacy of clopidogrel will be assessed by inter-group comparison on the VASP test. Study period: 7 days' treatment per patient. Total study period estimated at 6 months. Expected findings: The results should confirm the suspected negative effect of omeprazole on clopidogrel's impact on arterial thrombosis risk, secondarily allowing new recommendations to be drawn up for this association.
Detailed Description
Preventing recurrence of thrombosis following angioplasty relies on dual-therapy associating the anti-platelet agents aspirin and clopidogrel. This regime is kept up for between 1 and 6 months, depending on the type of stent deployed in the angioplasty. The biological effectiveness of the clopidogrel treatment can be assessed by the VASP test, a new platelet test, results on which have been shown to correlate with risk of thrombosis. A study we ran recently strongly suggested that omeprazole was associated with a poor response to clopidogrel. Omeprazole is an anti-ulcer agent frequently prescribed to prevent unwanted side-effects of aspirin, making it frequently associated to clopidogrel in the aftermath of angioplasty. Study population: 120 patients from the Cardiology Department of Brest University hospital, Brest (France), receiving a standard treatment comprising a loading dose of clopidogrel followed by a daily dose of 75 mg associated to 75 mg aspirin, will be randomized between 20 mg/day omeprazole and 20 mg/day placebo treatment groups. The efficacy of clopidogrel will be assessed by inter-group comparison on the VASP test. Study period: 7 days' treatment per patient. Total study period estimated at 6 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Heart Disease
Keywords
clopidogrel, omeprazole

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
120 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
impact on VASP test
Primary Outcome Measure Information:
Title
inter group comparison of VASP test

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patient with indication of aspirin and clopidogrel treatment Exclusion Criteria: patient<18 years liver disease drug eluting stent gastrointestinal ulcus bleeding pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
martine gilard, md
Organizational Affiliation
PI
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Cardiology
City
Brest
ZIP/Postal Code
29200
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
18206732
Citation
Gilard M, Arnaud B, Cornily JC, Le Gal G, Lacut K, Le Calvez G, Mansourati J, Mottier D, Abgrall JF, Boschat J. Influence of omeprazole on the antiplatelet action of clopidogrel associated with aspirin: the randomized, double-blind OCLA (Omeprazole CLopidogrel Aspirin) study. J Am Coll Cardiol. 2008 Jan 22;51(3):256-60. doi: 10.1016/j.jacc.2007.06.064.
Results Reference
derived

Learn more about this trial

Influence Of Omeprazole On The Anti-Platelet Action Of Clopidogrel

We'll reach out to this number within 24 hrs